ENST00000698728.1:n.1252T>A
|
|
|
ENST00000698729.1:n.2798T>A
|
|
|
ENST00000698730.1:n.2798T>A
|
|
|
ENST00000698731.1:c.1532T>A
|
ENSP00000513898.1:p.Phe511Tyr
|
|
ENST00000698732.1:c.*534T>A
|
ENSP00000513899.1:n.*534T>A
|
|
ENST00000698733.1:c.*860T>A
|
ENSP00000513900.1:n.*860T>A
|
|
ENST00000698734.1:c.1673T>A
|
ENSP00000513901.1:p.Phe558Tyr
|
|
ENST00000698735.1:n.1788T>A
|
|
|
ENST00000698736.1:n.1788T>A
|
|
|
ENST00000698737.1:n.1788T>A
|
|
|
ENST00000698738.1:n.1788T>A
|
|
|
ENST00000698739.1:n.1788T>A
|
|
|
ENST00000372371.8:c.1673T>A
MANE Select
|
ENSP00000361446.3:p.Phe558Tyr
|
|
ENST00000372371.7:c.1673T>A
|
ENSP00000361446.3:p.Phe558Tyr
|
|
ENST00000473588.2:c.475T>A
|
|
|
NM_007055.3:c.1673T>A
|
NP_008986.2:p.Phe558Tyr
|
|
NM_007055.4:c.1673T>A
MANE Select
|
NP_008986.2:p.Phe558Tyr
|
|